Aging and Apolipoprotein E in HIV Infection

Rebeca Geffin1, Micheline McCarthy2

  • 1Department of Neurology, University of Miami Miller School of Medicine, 1120 NW 14th St, Miami, FL, 33136, USA.

Insights

Effective antiretroviral therapy (ART) allows longer lifespans for people with HIV. However, aging and apolipoprotein E (ApoE) may accelerate brain aging and neurocognitive impairment in HIV patients.

Area of Science:

  • Neuroscience
  • Immunology
  • Gerontology

Background:

  • Antiretroviral therapy (ART) has transformed HIV infection into a chronic condition, increasing patient lifespan.
  • Despite ART, HIV-infected individuals experience accelerated aging, manifesting as organ-associated diseases and systemic syndromes similar to older, uninfected individuals.
  • HIV-associated neurocognitive disorders (HAND) represent a spectrum of neurological, cognitive, and motor deficits, potentially linked to accelerated aging mechanisms or superimposed comorbidities.

Purpose of the Study:

  • To review current evidence on the influence of aging on HIV-associated neurocognitive impairment.
  • To examine the role of apolipoprotein E (ApoE) in the development of HAND.
  • To understand the interaction between aging, ApoE, and cognitive function in the context of long-term HIV infection and ART.

Main Methods:

  • Literature review of recent studies on aging, ApoE, and HIV-associated neurocognitive disorders.
  • Analysis of evidence linking chronological age and biological aging processes to neurocognitive deficits in HIV.
  • Investigation of studies exploring the association between ApoE genotype and HAND prevalence and severity.

Main Results:

  • HIV infection, even with effective ART, is associated with accelerated brain aging and increased risk of neurocognitive impairment.
  • Comorbidities common in aging, coupled with chronic inflammation from HIV, exacerbate neurocognitive deficits.
  • The role of apolipoprotein E (ApoE) in HAND is debated, with conflicting evidence regarding its interaction with age to affect brain function in HIV patients.

Conclusions:

  • HIV-infected individuals are living longer, necessitating a focus on age-related health issues, including neurocognitive function.
  • Aging and ApoE are critical factors to consider when evaluating neurocognitive impairment in the growing population of long-term HIV survivors.
  • Further research is needed to clarify the complex interplay between aging, ApoE, and HAND to optimize management strategies.

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